Fonslow Bryan R, Yates John R
Department of Chemical Physiology, The Scripps Research Institute, La Jolla, CA 92037, USA.
J Sep Sci. 2009 Apr;32(8):1175-88. doi: 10.1002/jssc.200800592.
In the postgenomic era, proteomics has become a dominant field for identifying and quantifying the complex protein machinery of the cell. The expression levels, posttranslational modifications, and specific interactions of proteins control the biology of such processes as development, differentiation, and signal transduction. Studies of the proteins involved in these processes often lead to a better understanding of biology and of human disease. Powerful separation techniques and sensitive detection methods enable researchers to untangle these complicated networks of processes. CE coupled with either MS or LIF are two of the techniques that make this possible. This review will cover proven CE-based methods for proteomics on the cell and tissue level and their application in biological and clinical studies, relevant new developments in enabling technology such as microfluidic CE-MS demonstrated on model systems, and comment on the future of CE in proteomics.
在后基因组时代,蛋白质组学已成为识别和定量细胞中复杂蛋白质机制的主导领域。蛋白质的表达水平、翻译后修饰及特异性相互作用控制着诸如发育、分化和信号转导等过程的生物学特性。对参与这些过程的蛋白质进行研究往往有助于更好地理解生物学特性和人类疾病。强大的分离技术和灵敏的检测方法使研究人员能够梳理这些复杂的过程网络。毛细管电泳(CE)与质谱(MS)或激光诱导荧光(LIF)联用是实现这一目标的两种技术。本综述将涵盖已证实的基于CE的细胞和组织水平蛋白质组学方法及其在生物学和临床研究中的应用,在模型系统上展示的诸如微流控CE-MS等使能技术的相关新进展,并对CE在蛋白质组学中的未来发展进行评述。